Executive Director, Global Regulatory Submissions at Allergan
Irvine, California
Meredith Sewell is skilled in: Regulatory Submissions, Regulatory Affairs, eCTD, Pharmaceutical Industry, FDA, Sop, Documentum, Clinical Trials, IND, Biotechnology, GCP, Regulatory Requirements, 21 CFR Part 11, CTMS, Clinical Development, Document Management, Drug Development, Pharmacovigilance, SOP
Meredith Sewell is skilled in: Regulatory Submissions, Regulatory Affairs, eCTD, Pharmaceutical Industry, FDA, Sop, Documentum, Clinical Trials, IND, Biotechnology, GCP, Regulatory Requirements, 21 CFR Part 11, CTMS, Clinical Development, Document Management, Drug Development, Pharmacovigilance, SOP
What industry does Meredith Sewell work in?
Meredith Sewell works in the industry.
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